Canonical Allele Identifier: CA943861419
Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1939611399

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756870_134756871del , CM000673.2:g.134756870_134756871del GRCh38
NC_000011.9:g.134626764_134626765del , CM000673.1:g.134626764_134626765del GRCh37
NC_000011.8:g.134131974_134131975del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4204_599-4203del